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Pelubiprofen

CAT: 0804-HY-12383-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-12383-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Pelubiprofen is an orally active anti-inflammatory agent that inhibits COX enzyme activity (with IC50 values of 10.66 and 2.88 μM for COX-1 and COX-2, respectively) . Pelubiprofen has significant anti-inflammatory and analgesic effects[1][2].
CAS Number
69956-77-0
UNSPSC
12352005
Target
COX; IKK; MAP3K; NF-κB; NO Synthase
Type
Reference compound
Related Pathways
Immunology/Inflammation; MAPK/ERK Pathway; NF-κB
Applications
COVID-19-immunoregulation
Field of Research
Inflammation/Immunology; Neurological Disease
Assay Protocol
https://www.medchemexpress.com/pelubiprofen.html
Purity
99.27
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
O=C(O)C(C)C1=CC=C(/C=C2C(CCCC/2)=O)C=C1
Molecular Formula
C16H18O3
Molecular Weight
258.31
References & Citations
[1]Choi IA, Baek HJ, et al. Comparison of the efficacy and safety profiles of a pelubiprofen versus celecoxib in patients with rheumatoid arthritis: a 6-week, multicenter, randomized, double-blind, phase III, non-inferiority clinical trial. BMC Musculoskelet Disord. 2014 Nov 18;15:375.|[2]Ji-Sun Shin, et al. Anti-inflammatory effect of pelubiprofen, 2-[4- (oxocyclohexylidenemethyl) -phenyl]propionic acid, mediated by dual suppression of COX activity and LPS-induced inflammatory gene expression via NF-κB inactivation. J Cell Biochem. 2011 Dec;112 (12) :3594-603.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
COX-2; MAP3K7/TAK1

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